lisinopril - 54868-4657-7 - (lisinopril)

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Drug Information of lisinopril

Product NDC: 54868-4657
Proprietary Name: lisinopril
Non Proprietary Name: lisinopril
Active Ingredient(s): 10    mg/1 & nbsp;   lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of lisinopril

Product NDC: 54868-4657
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075994
Marketing Category: ANDA
Start Marketing Date: 20050725

Package Information of lisinopril

Package NDC: 54868-4657-7
Package Description: 270 TABLET in 1 BOTTLE (54868-4657-7)

NDC Information of lisinopril

NDC Code 54868-4657-7
Proprietary Name lisinopril
Package Description 270 TABLET in 1 BOTTLE (54868-4657-7)
Product NDC 54868-4657
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050725
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LISINOPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of lisinopril


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